List of variants in gene GRIN2B reported as uncertain significance by Baylor Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000834.5(GRIN2B):c.3004G>C (p.Gly1002Arg)	rs761281000	0.00001
NM_000834.5(GRIN2B):c.1306T>C (p.Cys436Arg)	rs1565478152
NM_000834.5(GRIN2B):c.1721TCTTTG[1] (p.574VF[1])	rs1555111511
NM_000834.5(GRIN2B):c.1783C>A (p.Pro595Thr)	rs766030730
NM_000834.5(GRIN2B):c.1937A>G (p.Tyr646Cys)	rs1565474582
NM_000834.5(GRIN2B):c.2071A>G (p.Thr691Ala)	rs1565457892
NM_000834.5(GRIN2B):c.2273_2281del (p.Ala758_Thr760del)	rs1565457062
NM_000834.5(GRIN2B):c.2450A>G (p.Asn817Ser)	rs1555103159
NM_000834.5(GRIN2B):c.2452A>G (p.Met818Val)
NM_000834.5(GRIN2B):c.2471T>G (p.Met824Arg)	rs1565455878
NM_000834.5(GRIN2B):c.4307G>C (p.Gly1436Ala)	rs1565452616

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